Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
  • C07F9/02—Phosphorus compounds
  • C07F9/28—Phosphorus compounds with one or more P—C bonds
  • C07F9/50—Organo-phosphines
  • C07F9/505—Preparation; Separation; Purification; Stabilisation
  • C07F9/5063—Preparation; Separation; Purification; Stabilisation from compounds having the structure P-H or P-Heteroatom, in which one or more of such bonds are converted into P-C bonds
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
  • C07F9/02—Phosphorus compounds
  • C07F9/28—Phosphorus compounds with one or more P—C bonds
  • C07F9/50—Organo-phosphines
  • C07F9/505—Preparation; Separation; Purification; Stabilisation
  • C07F9/5063—Preparation; Separation; Purification; Stabilisation from compounds having the structure P-H or P-Heteroatom, in which one or more of such bonds are converted into P-C bonds
  • C07F9/5068—Preparation; Separation; Purification; Stabilisation from compounds having the structure P-H or P-Heteroatom, in which one or more of such bonds are converted into P-C bonds from starting materials having the structure >P-Hal
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
  • C07F9/02—Phosphorus compounds
  • C07F9/28—Phosphorus compounds with one or more P—C bonds
  • C07F9/50—Organo-phosphines
  • C07F9/5031—Arylalkane phosphines
• • C—CHEMISTRY; METALLURGY
  • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
  • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
  • C25B3/00—Electrolytic production of organic compounds
  • C25B3/20—Processes
  • C25B3/25—Reduction

Definitions

• the invention relates to a process for preparing tertiary diarylalkylphosphines by reductive coupling of halodiarylphosphines with a quaternary ammonium compound, the reduction preferably proceeding via an electrochemical process.
• Tertiary phosphines in particular tertiary phosphines having bulky aromatic or araliphatic ligands, are used in a great variety of forms as ligands for complexing heavy metal atoms.
• the complexes thus obtained have achieved great importance as catalysts in a series of important industrial processes, e.g. hydrogenations and oxosyntheses.
• Tertiary diarylalkylphosphines can in principle be prepared by two different methods, generally starting from industrially available diarylphosphorus(III) compounds such as, for example, diarylchlorophosphines and forming a third P-C bond.
• a second known method comprises producing the metal salt of a diarylphosphine anion and reacting this with an alkyl halide.
• this process cannot be generally used:
• the European Patent EP 0 268 526 describes an electrochemical process for preparing tertiary diarylalkylphosphines, wherein the electrochemical reduction of arylhalophosphines is carried out in the presence of organic aliphatic halides in an electrolysis cell equipped with electrodes in an organic solvent medium containing an inert electrolyte and a consumable anode is used.
• This process gives satisfactory to good yields in the case of alkyl halides having pure alkyl radicals, e.g. n-butyl radicals, or even certain substituted alkyl radicals, but on the other hand moderate to poor yields in the case of araliphatic radicals (30% or 44% for benzyl chloride).
• Y, Z is (C 1 -C 4 )alkyl, hydrogen
• Aryl is phenyl, naphthyl, anthracenyl, phenanthrenyl or biphenyl, binaphthyl
• alkyl and cycloalkyl radicals can also be substituted by CN, O(C 1 -C 4 ) alkyl, CO(C 1 -C 4 ) alkyl, COO (C 1 -C 4 ) alkyl, --CH 2 --CH 2 --(C 1 -C 10 ) polyfluoroalkyl, where the cycloalkyl radicals can also contain --O or --S-moieties in the ring;
• the aryl radicals can be substituted by CN, halogen, CO (C 1 -C 4 ) alkyl, COO(C 1 -C 4 ) alkyl, --CH 2 --CH 2 --(C 1 -C 10 ) polyfluoroalkyl, a ##STR6## radical, R 2 , R 3 are, independently of one another, phenyl, naphthyl, anthracenyl, which can also be substituted by halogen, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy,
• R 4 , R 5 , R 6 are identical or different and are (C 1 -C 12 )alkyl or
• R 4 and R 5 together form a 5-membered or 6-membered ring which can, if desired, contain further N, O or S atoms in the ring,
• R 4 , R 5 and R 6 form a bicyclic ring system having nitrogen as bridge head atom and, if desired, further nitrogen, oxygen or sulphur atoms in the ring,
• X is bromine, chlorine, fluorine, (C 1 -C 4 ) alkoxy, O-phenyl,
• A is an anion of an organic or inorganic acid.
• R 1 is (C 1 -C 8 )alkyl, (C 3 -C 8 )cycloalkyl, CH 2 -phenyl, --CH 2 -naphthyl or CH 2 -biphenyl, where the phenyl, biphenyl and naphthyl radicals can be substituted by ##STR9## and R 2 , R 3 are phenyl or naphthyl, R 4 , R 5 , R 6 are (C 1 -C 10 )alkyl and X is bromine, chlorine or fluorine.
• the compounds of the formula (III) can be quaternary ammonium compounds having 4 identical radicals. If the starting compound has different radicals R 1 , R 4 , R 5 , R 6 , the radical R 1 to be transferred has to preferentially bond to the diphenylphosphine group. Examples which may be mentioned of the first group are: tetramethylammonium, tetraethylammonium, tetrapropylammonium or tetrabutylammonium salts.
• R 1 is always the first-named group: allyltrimethylammonium, benzyltrimethylammonium, N-benzyl-N-methylpiperidinium, N-benzyl-N,N'-dimethylpiperazinium, N-benzyl-N-methylmorpholinium, N-benzyl (diazabicyclo [2.2.2]octyl) ammonium, (2 -naphthylmethyl) triethylammonium, 4 - fluorobenzyltrimethylammonium, pentafluorobenzyltrimethylammonium, 2,6-dichlorobenzyltrimethylammonium, 2-cyanobenzyltrimethylammonium, 4-(trifluoromethyl)benzylammonium, cyclohexyltrimethylammonium or (carbomethoxymethyl)trimethylammonium salts.
• Bisquaternary ammonium compounds for example, 2,2'-bis[(trimethylammonio) methyl]biphenyl salts or 2,2'-bis [(trimethylammonio) methyl]-1,1'-binaphthyl salts can likewise be used as starting compounds of the formula (III).
• the reduction of the compounds of the formula (II) can be carried out in the presence of the ammonium compound of the formula (III), but it is also possible to carry out the reduction first and subsequently add the ammonium compound.
• diarylphosphines of the formula (II) is preferably carried out electrochemically, but can also be carried out by a chemical route, e.g. using metals, in particular alkali metals ("Methoden der organischen Chemie” (Houben Weyl), 4th edition (1963), volume XII/1, page 56).
• an undivided electrolysis cell which can be of any shape, for example a trough-shaped cell or a flow-through cell, and which has at least one cathode and one anode.
• the cathode comprises one of the usual metals, for example aluminum, magnesium, iron, nickel, chromium, titanium, copper, zinc, lead, cadmium, silver, gold or platinum or alloys of these metals, preferably chromium-nickel steel, or carbon materials, for example graphite or vitreous carbons.
• anode use is made of metals which are difficult to deposit cathodically under the electrolysis conditions, for example aluminum, calcium or preferably magnesium.
• Suitable electrolytes are aprotic, dipolar solvents, for example acetonitrile, dimethylacetamide, N-methylpyrrolidone, tetrahydrofuran or preferably dimethylformamide.
• an inert conductance salt which is soluble in the electrolyte can be additionally added to improve the electric conductivity, for example alkali metal or alkaline earth metal halides, for example sodium bromide or preferably magnesium chloride.
• the process of the invention is carried out at temperatures between about 0° C. and 80° C., preferably between 10° C. and 60° C.
• the electrolysis is carried out at current densities between about 1 and 100 mA/cm 2 , preferably between 5 and 50 mA/cm 2 .
• the electrolyte is advantageously moved relative to the electrodes by stirring or flow. If the reaction is carried out with the quaternary ammonium compound being added during the electrochemical reduction, the electrolyte can be stirred further for a certain time subsequent to the electrolysis to complete the conversion.
• the isolation of the process products is carried out in a manner known per se, for example by distilling off the solvent, dissolving the residue in a further water-immiscible solvent selected from the group consisting of hydrocarbons, halogenated hydrocarbons, ethers or ketones, extracting said solution with dilute mineral acid, evaporating the solvent and isolating the crude product obtained as residue by fractional distillation or crystallization.
• a further water-immiscible solvent selected from the group consisting of hydrocarbons, halogenated hydrocarbons, ethers or ketones
• the compounds of the formula (III) can be prepared by generally known methods, e.g. by reacting an alkyl halide with a tertiary amine ("Methoden der organischen Chemie” (Houben-Weyl), 4th edition (1963) , volume XI/2, page 593 ff.).
• 2,2,-bis[(trimethylammonium)methyl]-1,1'-binaphthyl dibromide can be prepared, for example, in virtually quantitative yield by reacting 2,2'-bis(bromomethyl)-1,1'-binaphthyl with trimethylamine in dimethylformamide at 70° C.
• the cell comprises a cylindrical glass vessel (diameter 40 mm; height 110 mm) fitted with a cooling jacket and a glass lid provided with a ground glass joint, in which lid there are located 5 smaller ground openings.
• the anode used is a magnesium rod (diameter 10 mm; length 100 mm; immersion depth about 55 mm)
• the cathode is a rectangular mesh of chromium-nickel steel (60 ⁇ 500 mm) which is shaped into a cylinder and is arranged concentrically around the anode (the spacing between the electrodes is about 3 mm).
• the electrodes are held in the lid of the cell by stiff wires of chromium-nickel steel which serve as power leads.
• the cell is further equipped with a thermometer, a gas inlet tube for nitrogen and a bubble counter. A further opening is closed by a septum of silicone rubber.
• the electrolyte is stirred by means of a magnetic bar.
• the dry cell is charged with 60 ml of dimethylformamide (max. 0.1% of water) and 10.51 g (0.050 mol) of tetraethylammoniumbromide. While stirring, a dry stream of nitrogen is passed through the mixture for 0.5 h, 8.82 g (0.040 mol) of chlorodiphenylphosphine are subsequently added and the electrolysis is commenced immediately afterwards with continued stirring and a passing through of a slow stream of nitrogen.
• the current is a constant 0.3 A, the temperature is from 35° to 40° C.
• the cell voltage is in the range from 0 to 1.5 volts.
• the amount of charge is 1.41 Ah.
• the electrolyte is stirred for a further 6 h at 50° C.
• the electrolyte contains 5.15 g of ethyldiphenylphosphine; this corresponds to a yield of 60% based on chlorodiphenylphosphine used.
• the product is isolated in the following way: The electrolyte is evaporated on a rotary evaporator at 70° C./20 mbar, the residue obtained is taken up in 150 ml of 1N hydrochloric acid and 50 ml of methylene chloride and stirred thoroughly; the methylene chloride phase is washed with 150 ml of water, dried over sodium sulphate and the methylene chloride is distilled off.
• Example 1 An electrolysis cell as described in Example 1 is used.
• the electrolyte comprises 60 ml of dimethylformamide (max. 0.1% of water), 16.12 g (0.050 mol) of tetra-n-butylammonium bromide and 8.82 g (0.040 mol) of chlorodiphenylphosphine.
• the electrolysis is carried out as described in Example 1. After the electrolysis, the electrolyte is stirred for a further 2 h at 35°-40° C.
• the electrolyte contains 6.96 g of n-butyldiphenylphosphine; this corresponds to a yield of 72% based on chlorodiphenylphosphine used.
• Workup and fractional distillation as described in Example 1 gives 4.78 g of 94%-pure product.
• the 31 P NMR spectrum and the 1 H NMR spectrum agree with an authentic sample.
• Example 1 An electrolysis cell as described in Example 1 is used.
• the electrolyte comprises 50 ml of dimethylformamide (max. 0.1% of water), 8.16 g (0,030 mol) of benzyltriethylammonium bromide and 5.52 g (0.025 mol) of chlorodiphenylphosphine.
• the amount of charge is 1.08 Ah.
• the electrolysis and workup of the electrolyte are carried out as described in Example 1. After evaporating the methylene chloride phase, there remain 6.60 g of residue which, according to analysis by gas chromatography (internal standard: 2-methylnaphthalene), contains 85% by weight of benzyldiphenylphosphine.
• the material yield based on chlorodiphenylphosphine used is 81%. Fractional distillation gives a 95%-pure product whose 31 P NMR spectrum agrees with an authentic sample.
• the electrolysis cell as described in Example 1 is used.
• the electrolyte comprises 50 ml of dimethylacetamide (max. 0.1% of water), 4.70 g (0,025 mol) of benzyltrimethylammonium chloride and 6.62 g (0,030 mol) of chlorodiphenylphosphine.
• the amount of charge is 0.96 Ah.
• the electrolysis is carried out at a current of 0.3 A and a temperature of 25° C.
• the electrolyte is subsequently stirred for a further 3 h at 35°-40° C.
• the electrolyte contains 5.47 g of benzyldiphenylphosphine in dissolved form, which can be isolated by workup as described in Example 1. The yield is 79% based on benzyltrimethylammonium chloride used.
• An electrolysis cell as described in Example 1 is used.
• the electrolyte comprises 50 ml of dimethylformamide (max. 0.1% of water) and 5.57 g (0,030 mol) of benzyltrimethylammoniumchloride.
• a total of 8.82 g (0.040 mol) of chlorodiphenylphosphine are added during the electrolysis in 4 equal portions: 2.2 g at the beginning of the electrolysis, 2.2 g after 0.32 Ah, 2.2 g after 0.64 Ah and 2.2 g after 1.34 Ah.
• the electrolysis is carried out with continued stirring and passage of a slow stream of nitrogen and a current of 0.3 A and a temperature of from 20° to 25° C.
• the electrolyte contains, according to analysis by gas chromatography (internal standard: 2-methylnaphthalene) 7.10 g of benzyldiphenylphosphine which can be isolated by workup as described in Example 1. The yield is 85% based on benzyltrimethylammonium chloride used.
• Example 1 An electrolysis cell as described in Example 1 is used.
• the electrolyte comprises 70 ml of dimethylformamide (max. 0.1% of water), 0.4 g of anhydrous magnesium chloride and 6.62 g (0.030 mol) of chlorodiphenylphosphine.
• the electrolysis is carried out as described in Example 1.
• the electrolysis temperature is 25° C. After an amount of charge of 0.96 Ah, the electrolysis is ended. 4.64 g (0.025 mol) of benzyltrimethylammonium chloride are then introduced into the electrolyte with exclusion of air and the mixture is stirred at 35° C.
• the reaction mixture contains, according to analysis by gas chromatography (internal standard: 2-methylnaphthalene), 5.72 g of benzyldiphenylphosphine (yield 83%, based on benzyltrimethylammonium chloride used) which can be isolated by workup as described in Example 1.
• Example 1 An electrolysis cell as described in Example 1 is used.
• the electrolyte comprises 50 ml of dimethylformamide (max. 0.1% of water), 0.4 g of anhydrous magnesium chloride and 6.62 g (0.030 mol) of chlorodiphenylphosphine.
• the electrolysis is carried out as described in Example 1.
• the electrolysis temperature is 25° C. After an amount of charge of 1.0 Ah, the electrolysis is ended. 5.58 g (0,010 mol) of 2,2'-bis[(trimethylammonio)methyl]-1,1'-binaphthyl dibromide are then introduced into the electrolyte under nitrogen and the mixture is stirred for 3 h at from 30° to 35° C. until a clear solution is formed.
• the workup is carried out as follows with exclusion of atmospheric oxygen:
• the electrolyte is evaporated on a rotary evaporator at 70° C./20 mbar, the residue obtained is taken up in 100 ml of 1N hydrochloric acid and 50 ml of methylene chloride and stirred thoroughly.
• the methylene chloride phase is washed with 100 ml of water, dried over sodium sulphate and the methylene chloride is evaporated under reduced pressure.
• the residue comprises 8.20 g of resinous solid. This residue is refluxed for about 1 h with 50 ml of isopropanol while stirring vigorously. In this way, the compact solid forms a finely divided, colorless product.
• Example 7 The procedure of Example 7 is repeated, but using an electrolyte comprising 5.58 g (0.010 mol) of 2,2'-bis[(trimethylammonio)methyl]-1,1'-binaphthyl dibromide, 6.62 g (0.030 mol) of chlorodiphenylphosphine and 50 ml of dimethyl formamide (max. 0.1% of water) in the electrolysis. The amount of charge is 0.96 Ah. Workup gives 5.1 g of 2,2'-bis[(diphenylphosphino)methyl]-1,1'-binaphthyl ("naphos"). This corresponds to a yield of 78% based on 2,2'-bis[(trimethylammonio)methyl]-1,1'-binaphthyl dibromide used.
• a dry 100 ml round-bottomed flask which is equipped with a magnetic stirrer bar, nitrogen inlet tube, bubble counter and a septum and has previously been flushed with dry nitrogen, is charged with 1.86 g (0.010 mol) of powdered benzyltrimethylammonium chloride and, by means of a syringe via the septum, 20 ml of a solution of 2.24 g (0.010 mol) of potassium diphenylphosphide in tetrahydrofuran (obtained as a ready-prepared 0.5M solution from Aldrich-Chemie GmbH & Co. KG, D-89555 Steinheim, Germany) at room temperature in one shot.
• the reaction mixture is stirred for a further 4 hours at room temperature, with the color gradually changing from red to yellow.
• the reaction mixture is mixed by stirring with 20 ml of 1N hydrochloric acid, the tetrahydrofuran phase is separated off, the aqueous phase is extracted twice with 10 ml of tetrahydrofuran and the two extracts are combined with the tetrahydrofuran phase.
• the combined tetrahydrofuran phases contained 2.50 g of benzyldiphenylphosphine; this corresponds to a yield of 90%.
• Example 9 An apparatus as described in Example 9 is used. After making inert with nitrogen, it is charged with 5.58 g (0.010 mol) of 2,2'-bis[(trimethylammonio)methyl]1,1'-binaphthyl dibromide and 44 ml of a solution of 4.93 g (0.022 mol) of potassium diphenylphosphide in tetrahydrofuran (as 0.5 M solution obtained ready-made from Aldrich-Chemie GmbH a Co, KG, D-89555 Steinheim, Germany) were added thereto while stirring over a period of about 5 minutes by means of a syringe. The temperature is from 20° to 30° C.
• reaction mixture is stirred for a further 3 h at room temperature and is then mixed with 20 ml of 1N hydrochloric acid, the tetrahydrofuran phase is separated off and the aqueous phase is extracted twice with 10 ml of tetrahydrofuran.
• the combined tetrahydrofuran phases are concentrated by distillation under reduced pressure.
• the residue is admixed with 50 ml of isopropanol and heated under reflux for i hour while stirring vigorously, the resinous material being converted into a colorless crystalline product. After cooling to room temperature, the product is filtered off with suction, washed 3 ⁇ with 10 ml each time of cold isopropanol and dried in a stream of nitrogen.

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• 1994
  • 1994-05-26 DE DE4418346A patent/DE4418346A1/de not_active Withdrawn
• 1995
  • 1995-04-22 TW TW084103986A patent/TW313570B/zh active
  • 1995-05-17 DE DE59509548T patent/DE59509548D1/de not_active Expired - Fee Related
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  • 1995-05-17 EP EP95107514A patent/EP0684248B1/de not_active Expired - Lifetime
  • 1995-05-23 AU AU20257/95A patent/AU681502B2/en not_active Ceased
  • 1995-05-24 KR KR1019950012964A patent/KR950032247A/ko not_active Abandoned
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  • 1995-05-25 CA CA002150207A patent/CA2150207A1/en not_active Abandoned
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